[go: up one dir, main page]

WO2002014318A8 - Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide - Google Patents

Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide

Info

Publication number
WO2002014318A8
WO2002014318A8 PCT/EP2001/008524 EP0108524W WO0214318A8 WO 2002014318 A8 WO2002014318 A8 WO 2002014318A8 EP 0108524 W EP0108524 W EP 0108524W WO 0214318 A8 WO0214318 A8 WO 0214318A8
Authority
WO
WIPO (PCT)
Prior art keywords
liquid crystalline
perylenetetracarboxylic acid
acid diimides
independently
applications
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2001/008524
Other languages
English (en)
French (fr)
Other versions
WO2002014318A1 (de
Inventor
Frank Wuerthner
Christoph Thalacker
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Priority to KR1020037001749A priority Critical patent/KR100845197B1/ko
Priority to AU2001289734A priority patent/AU2001289734A1/en
Priority to JP2002519458A priority patent/JP2004506635A/ja
Priority to US10/344,368 priority patent/US6806368B2/en
Priority to EP01969490A priority patent/EP1313735B1/de
Priority to DE50113895T priority patent/DE50113895D1/de
Publication of WO2002014318A1 publication Critical patent/WO2002014318A1/de
Publication of WO2002014318A8 publication Critical patent/WO2002014318A8/de
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
    • C09K19/60—Pleochroic dyes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/06—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
    • C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06—Non-steroidal liquid crystal compounds
    • C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3441—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
    • C09K19/3483—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom the heterocyclic ring being a non-aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00—Liquid crystal materials
    • C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
    • C09K19/60—Pleochroic dyes
    • C09K19/606—Perylene dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Indole Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Perylen-3,4:9,10-tetracarbonsäurediimide der allgemeinen Formel (I) mit folgender Bedeutung der Variablen: R?1, R2, R3 und R4¿ unabhängig voneinander Wasserstoff, Chlor, Brom oder gewünschtenfalls substituiertes Aryloxy, Arylthio, Arylamino, Hetaryloxy oder Hetarylthio; R?5, R6, R7, R8, R9 und R10¿ unabhängig voneinander Wasserstoff oder langkettiges Alkyl, Alkoxy oder Alkylthio, dessen Kohlenstoffkette jeweils bis zu vier Doppelbindungen enthalten kann, wobei mindestens vier dieser Reste von Wasserstoff verschieden sind, deren Herstellung und Verwendung als flüssigkristalline Materialien für elekronische, optoelektronische und photonische Anwendungen, zum Einfärben von hochmolekularen organischen und von anorganischen Materialien, als Fluoreszenzfarbstoffe und als Laserfarbstoffe sowie als organische Materialien für Solarkollektoren und Elektrolumineszenzanwendungen.
PCT/EP2001/008524 2000-08-11 2001-07-24 Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide Ceased WO2002014318A1 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
KR1020037001749A KR100845197B1 (ko) 2000-08-11 2001-07-24 액정 3,4:9,10-페릴렌테트라카르복실산 디이미드
AU2001289734A AU2001289734A1 (en) 2000-08-11 2001-07-24 Liquid crystalline 3,4:9,10-perylenetetracarboxylic acid diimides
JP2002519458A JP2004506635A (ja) 2000-08-11 2001-07-24 液晶性のペリレン−３，４：９，１０−テトラカルボン酸ジイミド
US10/344,368 US6806368B2 (en) 2000-08-11 2001-07-24 Liquid crystalline 3,4:9,10-perylenetetacarbocylic acid diimides
EP01969490A EP1313735B1 (de) 2000-08-11 2001-07-24 Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide
DE50113895T DE50113895D1 (de) 2000-08-11 2001-07-24 Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10039232A DE10039232A1 (de) 2000-08-11 2000-08-11 Flüssigkristalline Perylen-3,4:9,10-tetracarbonsäurediimide
DE10039232.6 2000-08-11

Publications (2)

Publication Number Publication Date
WO2002014318A1 WO2002014318A1 (de) 2002-02-21
WO2002014318A8 true WO2002014318A8 (de) 2002-06-27

Family

ID=7652091

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2001/008524 Ceased WO2002014318A1 (de) 2000-08-11 2001-07-24 Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide

Country Status (8)

Country Link
US (1) US6806368B2 (de)
EP (1) EP1313735B1 (de)
JP (1) JP2004506635A (de)
KR (1) KR100845197B1 (de)
CN (1) CN1239503C (de)
AU (1) AU2001289734A1 (de)
DE (2) DE10039232A1 (de)
WO (1) WO2002014318A1 (de)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000079617A1 (en) * 1999-06-21 2000-12-28 Cambridge University Technical Services Limited Aligned polymers for an organic tft
JP4678983B2 (ja) * 2001-05-14 2011-04-27 三井化学株式会社 有機電界発光素子
DE10218618A1 (de) * 2002-04-25 2003-11-06 Basf Ag Verfahren zur Herstellung von Perylen-3,4:9,10-tetracarbonsäuredimiden und Perylen-3,4:9,10-tetracarbonsäuredianhydrid sowie von Naphthalin-1,8-dicarbonsäureimiden
DE10225595A1 (de) * 2002-06-07 2003-12-18 Basf Ag 1,6,9,14-Tetrasubstituierte Terrylentetracarbonsäurediimide
DE10226181A1 (de) * 2002-06-12 2003-12-24 Basf Ag Verfahren zur Überführung von Perylen-3,4:9,10-tetracarbonsäurediimide in eine für die Anwendung als Fluoreszenzfarbmittel geeignete Form
GB0312067D0 (en) * 2003-05-24 2003-07-02 Avecia Ltd Inks
CA2554302C (en) * 2004-01-26 2013-03-26 Northwestern University Perylene n-type semiconductors and related devices
DE102004018547A1 (de) * 2004-04-14 2005-02-03 Basf Ag Verfahren zum Schweißverbinden von Kunststoffteilen mit Hilfe von Laserstrahlung
DE102005018241A1 (de) * 2005-04-19 2006-10-26 Basf Ag Hexarylen- und Pentarylentetracarbonsäurediimide
CN1315829C (zh) * 2005-05-10 2007-05-16 山东师范大学 1，7－二取代－3，4∶9，10－苝双二酰亚胺的合成方法
CN100340558C (zh) * 2005-10-17 2007-10-03 东南大学 N,n＇－二吡啶基－3,4,9,10－苝四甲酰二亚胺衍生物及其合成方法
DE102005053995A1 (de) * 2005-11-10 2007-05-24 Basf Ag Verwendung von Rylenderivaten als Photosensibilisatoren in Solarzellen
WO2007093643A1 (de) 2006-02-17 2007-08-23 Basf Se Fluorierte rylentetracarbonsäurederivate und deren verwendung
EP1843407A1 (de) * 2006-04-07 2007-10-10 Basf Aktiengesellschaft Flüssig-kristalline Rylentetracarbonsäurederivate und deren Verwendung
US20070259475A1 (en) * 2006-05-04 2007-11-08 Basf Aktiengesellschaft Method for producing organic field-effect transistors
EP2022105B1 (de) 2006-05-04 2011-08-10 Basf Se Verfahren zum herstellen organischer feldeffekttransistoren
WO2007146250A2 (en) * 2006-06-12 2007-12-21 Northwestern University Naphthalene-based semiconductor materials and methods of preparing and use thereof
US20080054258A1 (en) * 2006-08-11 2008-03-06 Basf Aktiengesellschaft Use of perylene diimide derivatives as air-stable n-channel organic semiconductors
WO2008051552A2 (en) * 2006-10-25 2008-05-02 Northwestern University Organic semiconductor materials and methods of preparing and use thereof
JP5380296B2 (ja) * 2006-11-17 2014-01-08 ポリエラ コーポレイション ジイミド系半導体材料ならびにジイミド系半導体材料を調製および使用する方法
WO2008063583A1 (en) * 2006-11-17 2008-05-29 Polyera Corporation Acene-based organic semiconductor materials and methods of preparing and using the same
WO2008067445A2 (en) * 2006-11-29 2008-06-05 Sun Chemical Corporation Poly(oxyalkylene)ated colorants and their use as fluorescent security taggants
KR20090117730A (ko) * 2007-01-08 2009-11-12 폴리에라 코퍼레이션 아렌-비스(디카르복스이미드)-기재 반도체 물질, 및 이를 제조하기 위한 관련된 중간체의 제조 방법
WO2008091670A2 (en) * 2007-01-24 2008-07-31 Polyera Corporation Organic semiconductor materials and precursors thereof
JP5504180B2 (ja) * 2008-03-07 2014-05-28 日東電工株式会社 リオトロピック色素化合物、液晶系および光学異方性フィルム
US9701784B2 (en) 2008-03-26 2017-07-11 Yeda Research And Development Co. Ltd. Supramolecular polymers derived from perylene-diimides
US8968886B2 (en) 2008-03-26 2015-03-03 Yeda Research And Development Co., Ltd. Doubly reduced perylene-diimides and supramolecular polymers derived from perylene-diimides
KR101040729B1 (ko) 2008-05-22 2011-06-13 서울대학교산학협력단 페릴렌 단위를 포함하는 수용성 적색염료 화합물, 그제조방법, 이를 포함한 잉크 조성물 및 컬러필터
US8299354B2 (en) * 2008-08-19 2012-10-30 Sabic Innovative Plastics Ip B.V. Luminescent solar collector
US8304647B2 (en) * 2008-08-19 2012-11-06 Sabic Innovative Plastics Ip B.V. Luminescent solar collector
US8314325B2 (en) * 2008-08-19 2012-11-20 Sabic Innovative Plastics Ip B.V. Luminescent solar collector
US8304645B2 (en) * 2008-08-19 2012-11-06 Sabic Innovative Plastics Ip B.V. Luminescent solar collector
KR101012542B1 (ko) * 2008-12-12 2011-02-07 재단법인대구경북과학기술원 고분자 화합물 및 그를 포함하는 태양전지
US8486708B2 (en) 2009-01-30 2013-07-16 University Of Utah Research Foundation Perylene nanofiber fluorescent sensor for highly sensitive and selective sensing of amines
WO2010099214A1 (en) * 2009-02-27 2010-09-02 Nitto Denko Corporation Lyotropic chromophoric compounds, liquid crystal systems and optically anisotropic films
WO2011022141A1 (en) * 2009-08-20 2011-02-24 Nitto Denko Corporation Method of synthesizing core-expanded perylene diimide dye and novel core-expanded perylene diimide dye
WO2011079296A2 (en) 2009-12-23 2011-06-30 University Of Utah Photoconductive sensor materials for detection of explosive vapor
US8283469B2 (en) * 2010-03-24 2012-10-09 National Tsing Hua University Perylene diimide derivative and organic semiconductor element using the same material
EP2608874A1 (de) 2010-08-27 2013-07-03 Yeda Research and Development Co. Ltd. Trennung von nanopartikeln
US9623381B2 (en) 2010-08-27 2017-04-18 Yeda Research And Development Co. Ltd. Separation of nanoparticles
JP5775587B2 (ja) * 2010-09-10 2015-09-09 オーシャンズ キング ライティング サイエンス アンド テクノロジー シーオー．，エルティーディー ペリレンテトラカルボン酸ジイミド有機半導体材料、及び、その調合法
US9287419B2 (en) 2011-01-05 2016-03-15 Nitto Denko Corporation Wavelength conversion perylene diester chromophores and luminescent films
CN105419379B (zh) 2011-09-26 2018-11-20 日东电工株式会社 用于提高的日光采集效率的高荧光且光稳定性生色团
JP2013084952A (ja) 2011-10-05 2013-05-09 Nitto Denko Corp 太陽光捕集効率を向上させるための、感圧接着剤層を含む波長変換膜
CN105461628B (zh) * 2014-07-07 2020-05-15 江苏和成新材料有限公司 苯并菲-苝单酰亚胺二甲酸酯二元化合物及其制备方法及应用
KR101992009B1 (ko) * 2017-02-03 2019-06-21 동우 화인켐 주식회사 자발광 감광성 수지 조성물, 이를 이용한 색변환층을 포함하는 컬러필터 및 화상표시장치
CN109096790B (zh) * 2018-10-18 2020-11-24 西南科技大学 一种苝红染料苝红620的合成方法
CN110003207A (zh) * 2019-03-04 2019-07-12 天津大学 一类湾位苯氧基取代的苝酰亚胺荧光染料及其制备方法
CN111909150B (zh) * 2020-06-05 2022-05-10 北京文海阳工贸有限责任公司 一种近红外荧光染料及其在制备化学近红外辐射剂中的应用
KR102401913B1 (ko) * 2021-06-11 2022-05-25 최돈수 유기 전기 발광 소자용 발광 재료, 이를 이용한 유기 전기 발광 소자 및 유기 전기 발광 소자용 재료
CN116606293A (zh) * 2023-04-03 2023-08-18 中国船舶集团有限公司第七一八研究所 一种基于苝酰亚胺结构的化合物及其制备方法和应用

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3294778A (en) * 1964-09-14 1966-12-27 Gen Aniline & Film Corp Fiber-reactive dyestuffs
US3554776A (en) * 1967-11-24 1971-01-12 Allied Chem Novel perylenetetracarboxylic diimide compositions
DE3016764A1 (de) * 1980-04-30 1981-11-05 Heinz Dr. 5880 Lüdenscheid Langhals Verfahren zur erhoehung der loeslichkeit aromatischer systeme
US4378302A (en) * 1980-12-16 1983-03-29 General Electric Company Red perylene dichroic dye containing liquid crystal formulations
DE3110955A1 (de) 1981-03-20 1982-09-30 Basf Ag, 6700 Ludwigshafen Elektrophotographisches aufzeichnungsmaterial
DE3934329A1 (de) 1989-10-13 1991-04-18 Basf Ag Polymerisierbare perylen-3,4,9,10-tetracarbonsaeurebisimide sowie deren polymerisate
EP0697027B1 (de) 1993-05-04 1997-07-02 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Tetraaroxyperylen-3,4,9,10-tetracarbonsäurepolyimide
DE19547209A1 (de) 1995-12-18 1997-06-19 Basf Ag 1,7-Diaroxy-oder -arylthiosubstituierte Perylen-3,4,9,10-tetracarbonsäuren, deren Dianhydride und Diimide
DE19620746A1 (de) 1996-05-23 1997-11-27 Hoechst Ag Farbige Monomere enthaltende chirale cLCPs

Also Published As

Publication number Publication date
EP1313735A1 (de) 2003-05-28
CN1446219A (zh) 2003-10-01
EP1313735B1 (de) 2008-04-23
JP2004506635A (ja) 2004-03-04
KR20030020448A (ko) 2003-03-08
DE10039232A1 (de) 2002-02-21
KR100845197B1 (ko) 2008-07-10
US6806368B2 (en) 2004-10-19
DE50113895D1 (de) 2008-06-05
AU2001289734A1 (en) 2002-02-25
CN1239503C (zh) 2006-02-01
WO2002014318A1 (de) 2002-02-21
US20030181721A1 (en) 2003-09-25

Similar Documents

Publication Publication Date Title
WO2002014318A8 (de) Flüssigkristalline perylen-3,4:9,10-tetracarbonsäurediimide
Poddar et al. Recent advances of BODIPY based derivatives for optoelectronic applications
Chen et al. Optimization of opto‐electronic property and device efficiency of polyfluorenes by tuning structure and morphology
Huang et al. Designing transmitter ligands that mediate energy transfer between semiconductor nanocrystals and molecules
CA2200807A1 (en) Hydroxyphenyltriazines
KR20170003635A (ko) 시안화 페릴렌 화합물
EP1142895A4 (de) Borderivate und organische elektrolumineszierende verbindungen
WO2004003102A3 (en) Polymerizable, luminescent compounds and mixtures, luminescent polymer materials and their use
EP1138744A4 (de) Organische elektrolumineszente vorrichtung
KR20130113263A (ko) 신규한 유기 전기 발광 소자용 재료 및 이를 포함하는 유기전기발광소자
DE50008689D1 (en) Thermochrome rylenfarbstoffe
WO2002068538A3 (de) Thermochrome rylenfarbstoffe
WO2019031524A1 (ja) 蓄光組成物、蓄光素子および波長制御方法
DE50209795D1 (de) Lichtkoppelelement
ES2099024A1 (es) Nuevos derivados de 2,2,6,6-tetrametil-4-piperidinol para su uso como estabilizantes a la luz, estabilizantes al calor, y estabilizantes a la oxidacion para materiales organicos.
Li et al. Low-cost and stable SFX-based semiconductor materials in organic optoelectronics
US6461543B2 (en) Chemiluminescent solution based on disubstituted perylene tetracarboxylic acids, their dianhydrides and diimides
Arrigo et al. Highly efficient luminescent solar concentrators based on BODIPY derivatives
CN108276335A (zh) 一种含氮杂环衍生物及其有机发光器件
CN107674060A (zh) 一种芳香族胺类衍生物及其有机发光器件
MXPA94005411A (es) Compuestos novedosos de piperidina para utilizarsecomo estabilizantes para materiales organicos.
Aksoy Recycling of Waste Polymethyl-Methacrylate as an Optical Transparent Host
Eyal et al. SPECTROSCOPIE OF LASER DYE OXAZINE-170 AS A FUNCTION OF ENVIRONMENT AND pH
Mou et al. A class of fascinating optoelectronic materials: Triarylboron compounds
TW200710169A (en) Cyanine coloring matter and optical recordingMEDIUM

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
AK Designated states

Kind code of ref document: C1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: C1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

WR Later publication of a revised version of an international search report
WWE Wipo information: entry into national phase

Ref document number: 2001969490

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 1020037001749

Country of ref document: KR

Ref document number: 2002519458

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 018140475

Country of ref document: CN

Ref document number: 10344368

Country of ref document: US

WWP Wipo information: published in national office

Ref document number: 1020037001749

Country of ref document: KR

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 2001969490

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 2001969490

Country of ref document: EP